Evidence map›Paper›PMID 36291431›Full record

ArticleChildren (Basel, Switzerland)2022

Compound Heterozygous Missense Variants in

Bibhuti B Das, Viswanath Gajula, Sandeep Arya, Mary B Taylor

Open access · goldAbstract readCase Reports
In one paragraph

Article in Children (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Chromatin topology control by a muscle-specific ribosomal protein.bioRxiv : the preprint server for biology · 2026
    Article
  2. Infantile dilated cardiomyopathy caused by RPL3L gene mutation: A case report.The Journal of international medical research · 2026
    Article
  3. Article
  4. Understanding inherited cardiomyopathies: clinical aspects and genetic determinants.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2025
    Article
  5. Review
  6. RNA binding proteins in cardiovascular development and disease.Current topics in developmental biology · 2024
    Article
  7. Article
  8. Review
  9. Frontiers in physiology · 2023
    Article
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Bibhuti B DasDepartment of Pediatrics, Division of Cardiology, Children's of Mississippi, University of Mississippi Medical Center, Jackson, MS 39216, USA.ORCID 0000-0001-9530-8785
Viswanath GajulaDepartment of Pediatrics, Division of Critical Care, Children's of Mississippi, University of Mississippi Medical Center, Jackson, MS 39216, USA.ORCID 0000-0003-2786-0038
Sandeep AryaDepartment of Pediatrics, Division of Critical Care, Children's of Mississippi, University of Mississippi Medical Center, Jackson, MS 39216, USA.ORCID 0000-0001-7195-6067
Mary B TaylorDepartment of Pediatrics, Division of Critical Care, Children's of Mississippi, University of Mississippi Medical Center, Jackson, MS 39216, USA.
University of Mississippi Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole exome sequencing has identified an infant girl with fulminant dilated cardiomyopathy (DCM), leading to severe acute heart failure associated with ribosomal protein large 3-like (

Indexed as

familial dilated cardiomyopathypediatric heart failureRPL3L

Identifiers

PMID36291431
PMCPMC9600237
OpenAlexW4297973528

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.